NM_000719.7(CACNA1C):c.5139C>T (p.Asp1713=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 25, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000079295.7
Allele description [Variation Report for NM_000719.7(CACNA1C):c.5139C>T (p.Asp1713=)]
NM_000719.7(CACNA1C):c.5139C>T (p.Asp1713=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024